CA2333475C - Derivatives of pyrazolines, their preparation and their application as medicaments - Google Patents

Abstract

The present invention relates to new pyrazoline derivatives having the gener al formula (I), as well as to their physiologically acceptable salts, to process in human/veterinary therapy and to pharmaceutical compositions containing them. The new compounds of the invention can be used in the pharmaceutical industry as imtermediates and for the preparation of medicaments. In particular, they can be used for the preparation of medicaments used for the treatment of inflammation and other troubles associated to inflammation and other process mediated by cyclooxygenase-2, for example arthritis, pain treatment or fever treatment.

Description

^' . , .27395-101 DERIVATIVES OF PYRAZOLINES, THEIR PREPARATION AND
THEIR APPLICATION AS MEDICAMENTS

Field of the invention The present invention relates to new pyrazoline derivatives, of general formula (I), and to physiologically acceptable salts thereof, to the procedures for their preparation, to their application as medicaments in human and/or veterinary therapy and to the pharmaceutical compositions that contain them.

:;>':

(~) The new compounds of the present invention can be used in the pharmaceutical industry as intermediates and for the preparation of medicaments.
Background of the invention Non-steroid anti-inflammatory drugs (NSAIDS) are traditionally classified as anti-inflammatory, antipyretic and analgesic agents for the symptomatic alleviation of inflammation, fever and light to moderate pain. The main indications for these drugs are osteoarthritis, rheumatoid arthritis and other inflammatory diseases of articulations, as well as for the treatment of inflammations associated with small lesions and as analgesics of broad use. The NSAIDS are essentially inhibitors of acute inflammatory response, but in rheumatic disorders they have little effect on the underlying degenerative changes occurring in tissue.
The discovery of the main mechanism of action of the NSAIDS by inhibition of cyclooxygenase (COX) [J.R. Vane, Nature, 1971, 231, 232] provided a

2 satisfactory explanation of their therapeutic action and established the importance that certain prostaglandins have as mediators in inflammatory disease [R.J.
Flower, J.R. V'ane, Biochem. Pharm., 1974, 23, 1439; J.R. Vane, R.M. Botting, Postgrad Med. J., 1990, 66 (Suppl 4), S2] The gastric toxicity of the classic NSAIDS, as well as their beneficial effects, is due to the suppression of prostagiandin synthesis by inhibition of the COX enzyme. Although several strategies have been followed (enteral coating to prevent adsorption in the stomach, parenteral administration, pro-drug formulation, etc) to reduce the gastrointestinal lesions provoked by the NSAIDS, none of these modifications '10 have provided a significant impact on the incidence of serious adverse reactions such as perforation and haemorrhaging.
The discovery of an induced prostaglandin-synthetase, denominated cyclooxygenase-2 (COX-2), different from the constitutive enzyme, currently denominated cyclooxygenase-1 (COX-1 i[J. Sirois, J.R. Richards, J. Biol.
Chem., 1992, 267, 6382], has renewed the interest in the development of new anti-inflammatory drugs. The identification of the isoform COX-2 has led to the hypothesis that it could be responsible for the production of prostaglandins in places where inflammation occurs. As a result, selective inhibition of this isoenzyme would reduce the inflammation without producing the side effects of gastric and renal toxicity. Ttie COX-1 isoenzyme is essentially expressed in most of tissues with the function of synthesising prostaglandins which regulate the normal cell activity. On the other hand, the isoenzyme COX-2 is not normally present in cells but in chronic inflammation the levels of the protein COX-2 increase in parallel with the over-production of prostagiandins [J.R. Vane, R.M.
Botting, Inflamm. Res., 1995, 44, 1]. Therefore, a selective COX-2 inhibitor has the same anti-inflammatory, antipyretic and analgesic properties as a conventional non-steroid ariti-inflammatory agent and also inhibits the uterine contractions induced by hormones and presents potential anti-carcinogenic effects and beneficial effects in the prevention of the development of Alzheimer disease. On the other hand, a selective COX-2 inhibitor reduces the potential

3 gastrointestinal toxicity, reduces the potential renal side effects and reduces the effects of bleeding time.
The tri-dimensional structure of COX-1 has been determined by x-ray diffraction (D. Picot, a.J: Lc!!, R.M. Garavito, Nature, 1994, 367, 243].
Three of the helixes of the structure form the entrance to the cyclooxygenase chanriel and its insertion in the membrane allows the arachidonic acid to access the active site from inside the bilayer. The active site of cyclooxygenase is a large hydrophobic channel and the authors argue that the NSAIDS inhibit COX-1 by excluding arachidonic acid from the upper part of the channel. Recently [R.S. Service, Science, 1996 273, 1660], the three-dimensional structure of COX-2 has been described, which allows comparison of the similarities and differences between the two isoforms and therefore study of new drugs that selectively inhibit COX-2.
The structures of COX-1 and COX-2 show that the sites where the anti-inflammatory agents bind to the enzymes are very similar but there is a difference '15 of at least one important amino acid. A voluminous isoleucine present in the active site of COX-1 is replaced by a valine in COX-2. The isoleucine blocks the lateral cavity that is separated from the principle bond of both isoenzyrnes.
The blocked cavity of COX-1 does not impede the binding of classic NSAIDS, but an inhibitor that needs the extra support point supplied by the lateral cavity will bind more easily to COX-2 than to COX-1. As a result, a model for a new generation of anti-inflammatory agents is one where the inhibitors of cyclooxygenase have a large preference for the lateral cavity of COX-2 In the chemical literature derivatives of nitrogenated heterocyclic aromatics of five members have been described with COX-2 inhibitory activity. Within these azole derivatives are the pyrrols [W.W. Wilkerson, et al, J. Med. Chem., 1994, 37, 988; W.W. Wilkerson, et al, J. Med. Chem., 1995, 38, 3895; I.K. Khanna, et al, J.
Med. Chem., 1997, 40, 1619], pyrazoles [T.D. Penning, et al, J. Med. Chem., 1997, 40, 1347; K. Tsuji, et a!, Chem. Pharm. Bull., 1997, 45, 987; K. Tsuji, et a/, Chem. Pharm. Bull., 1997, 45, 1475], or imidazoles [Khanna, et al, J. Med.
Chem., 1997, 40, 1634].

4 We have now discovered that the novel compounds derived from pyrazolines of general formula (I) show interesting biological properties and these make them particularly useful for their employment in human and/or veterinary therapy. The compounds object of this invention are useful as agents with anti-inflammatory activity and for other diseases wherein cyclooxygenase-2 plays a part, without having the gastric and renal toxicity of the classic NSAIDS.

Detailed description of the invention The present invention provides new pyrazolines that inhibit the enzyme cyclooxygenase-2, with application in human and/or veterinary medicine as anti-inflammatories and for other diseases wherein cyclooxygenase-2 plays a part, and that have low or no gastric and renal toxicity. These anti-inflammatories therefore have a better safety profile. The new compounds object of the present '15 invention are derivatives of A 2-pyrazolines, also known as 4,5-dihydro-1 H-pyrazoles. They are therefore non-aromatic nitrogenated heterocyclic compounds.
As a result the pyrazoline rings are not planar as opposed to the azoles described previously. The compounds object of the present inventiori have the general formula (1) R R
N~.N
::2:

wherein R, represents an hydrogen atom, a methyl, fluoromethyl, difluoromethyl, trifluoromethyl, carboxylic acid, lower carboxylate of I to 4 carbon atoms, carboxamide or cyano group, R2 represents a hydrogen atom or methyl group, R3, R4, R, and R8i identical or different, represent an atom of hydrogen, chlorine or fluorine, a methyl, trifluoromethyl or methoxy group, one of RS 'and R6 represents an atom of hydrogen, chlorine w,fiucri^c,

5 a methyl, trifluoromethyl, methoxy or trifluoromethoxy group, and the other of R5 and R6 is a methylsulphonyl, aminosulphonyl or acetylaminosulphonyl group;
with the proviso that when R, represents a methyl group, then:
R2 represents a hydrogen atom or a methyl group, R3 and R8, identical or different, represent an atom of hydrogen,.
chlorine or fluorine, a methyl or trifluoromethyl group, R4 represents a hydrogen or fluorine atom, a methyl, trifluoromethyl or methoxy group, R5 represents a fluorine atom, trifluoromethyl, trifluoromethoxy, rrieVhylsulfonyl or aminosulphonyl group, R6 represents a hydrogen, chlorine., fluorine atom, a methyl, trifluoromethyl, , methoxy, trifluoromethoxy, methylsulfonyl or aminosulphonyl group, with the proviso that one of both R5 and R6 represents a methylsulfonyl or aminosulphonyl group; and R7 represents a hydrogen, chlorine or fluorine atom, a methyl, trifluoromethyl or methoxy group.
The new compounds of general formula (1) have an asymmetric carbon atom and so can be prepared enantiomerically pure or as racemates. The racemates of compounds (!) can be resolved into their optical isomers by conventional methods, such as separation by chiral stationary phase chromatography for example, or by fractionated crystallisation of their diastereoisomeric salts, which can be prepared by reacting the compounds (I) with enantiomerically pure acids.
Similarly, 'they can also be obtained by enantioselective synthesis using enantiomerically pure chiral precursors.
The present invention also relates to the physiologically acceptable salts of the compounds of general formula (I), in particular, to the addition. salts fdrmed

6 with mineral acids such as hydrochloric, hydrobromic, phosphoric, sulphuric, nitric acid, etc, and with organic acids such as citric, maleic, fumaric acid, tartaric acids or its derivatives, p-toluenesulphonic, rnethanosulphonic, camphosulphonic acid etc.
The novel derivatives of general formula (I) can be used in mammals, including man, as anti-inflammatory agents for the treatment of inflammation and for the treatment of other disorders associated with inflammation, such as analgesics for the treatment of pain and migraine, and as anti-pyretics in the treatment of fever. For example, the new derivatives of general formula (I) can be '10 used in the treatment of arthritis, including but limited to the treatment of rheumatoid arthritis, spondyloarthropathies, gouty arthritis, systemic lupus erythematosus, osteoarthritis and juvenile arthritis. The novel derivatives of general formula (I) can be used in the treatment of asthma, bronchitis, rnenstrual disorders, teridinitis, bursitis and different states that affect the skin such as psoriasis, eczema, burns and dermatitis_ The novel derivatives of general formula (I) can also be used in the treatment of gastrointestinal afflictions such as syndrome of inflamed intestine, Crohn's disease, gastritis, irritated colon syndrome and ulcerous colitis.
The novel derivatives of general formula (I) can be prepared, in accordance with the invention, following the methods that are indicated below:

Method A
The preparation of the compounds of general formula (I) is carried out by reacting a compound of general formula (II) R3 z

7 111) wherein R, represents an hydrogen atorri, a methyl, fluoromethyl, difluoromethyl, trifluoromethyl or carboxylic acid group, and R2, R3, R4 and R5 have the same meaning as that indicated for general formula (I), with a phenylhydrazine of general formula (III) in base or salt form R8 ~
~~

(III) wherein R6, R7 and R8 have the same meaning as that described previously for general formula I.
The reaction is carried out in the presence of a suitable solvent such as, for example, alcohols such as methanol, ethanol, ethers such as dioxane, tetrahydrofuran, or mixtures thereof or other solvents. The reaction takes place in acid medium, that can be organic, such as acetic acid, for example, or inorganic such as hydrochloric acid for example, or a mixture of both, or in a base medium such as piperidine, piperazine, sodium hydroxide, potassium hydroxide, sodium methoxide or sodium ethoxide for example, or a mixture thereof. The acidic or base medium itself can act as a solvent. The most suitable temperatures vary between room temperature and the reflux temperature of the solvent and the reaction times can lie between several ho-.irs and several days.

METHOD B
The preparation of the compounds of general formula (I), wherein R, represents a carboxylate of a lower alkyl with 1 to 4 carbon atoms and R2, R3, R4, R5, R6, R7 and R8 have the same meaning as that given above, is effected by

8 reacting a compound of generai formula (I) wherein R, represents a carboxylic acid group (COOH) and R2, R3, Ra1 R5, R6, R7 and R8 have the same meaning as that given above, with a suitable reagent to form the acid chloride such as thionyl chloride or oxalyl chloride for example, and then carrying out an esterification reaction with an aliphatic alcohol of 1 to 4 carbon atoms in the presence of an organic base, such as triethylamine or pyridine, or by direct reaction of carboxylic acid with the corresponding anhydrous alcohol saturated with gaseous hydrogen chloride. The reaction is carried out in the reagent as its own solvent or in other appropriate solvents such as halogenated hydrocarbons such as dichloromethane, chloroform or carbon tetrachloride, ethers such as dioxane, tetrahydrofuran, ethyl ether or dimethoxyethane. The most appropriate temperatures vary between 00 C and the reflux temperature of the solvent and the reaction times lie between ten minutes and 24 hours.

METHOD C
The preparation of the compounds of general formula (I), wherein R, represents a carboxamide group and R2, R3, R4, R5, R6, R7 and R8 have the same meaning as that indicated above, is carried out be reacting a compound of general formula (I) wherein F2, represents a carboxylic acid group (COOH) and R2, R3, R4, R5, R6, R7 and R8 have the same meaning as that indicated above, with a suitable reagent for forming the corresponding acid chloride, for example, thionyl chloride or oxalyl chloride arid then reacting with ammonia, that can be in the form of concentrated aqueous solution or dissolved in a suitable solvent. The reaction is carried out in a suitable solvent such as, for example, ethers such as dioxane, tetrahydrofuran, ethyl ether or dimethoxyethane. The most suitable temperatures vary between 00 C and the reflux temperature of the solvent and the reaction times lie between 1 and 24 hours.

METHOD D
The preparation of the compounds of general formula (I), wherein R, represents a cyano group and R2, R3, R4, R5, R6, R7 and R8 have the same

9 meaning as that indicated above, is carried out by reacting a compound of general formula (I) wherein R, represents a carboxamide group and R2, R3, R4, R5, R6, R7 and R8 have the same meaning as that indicated above, with a suitable reagent such as, for exa;npie, the complex dimethylformamide-thionyl chloride or methanosulphonyl chloride. The reaction is carried out in a suitable solvent such as, for example, dimethylformamide or pyridine. The most suitable temperatures vary between 01 C and the reflux temperature of the solvent and the reaction times lies between fifteen minutes and 24 hours.

METHOD E
The compounds of general formula (II), intermediates in the preparation of the compounds of general formula (I), are commercially available or can be obtained using different known methods among which the following are found:

The preparation of the compound of general formula (I!), wherein R, represents a mono- di- or trifluoromethyl group, R2 represents an hydrogen atom and R3, R4 and R5 have the same meaning indicated above for the compounds of general formula (I), is carried out by reaction of a benzaldehyde of general formula (IV) CHO
R3 ~

(IV) :30 wherein R3, R4 and RS have the same meaning as that given above for the general formula (I), with N-phenyl(mono, di or trifluoro)acetimidoyl chloride in the presence of a dialkyl phosphonate, such as phosphonate of diethylmethyl, and a strong organic base, such as LDA (lithium diisopropylamide), or by the Wittig reaction with mono-, di- or trifiuoroacetylmethylenetriphenylphosphorane and a base such as sodium carbonate or potassi um catwonate. The reaction is carried 5 out in a suitable solvent such as, for example, dichloromethane, chloroform or benzene, or an ether such as tetrahydrofuran, ethyl ether, dimethoxyethane or dioxane. The most suitable temperatures vary between -70 C and the reflux temperature of the solvent, and the reaction times lie between fifteen minutes and twenty hours.
METHOD E-2 The preparation of the compounds of general formula (!I), wherein R, represents a methyl or trifluoromethyl group, R2 represents a methyl group and R3, R4 and R5 have the same meaning indicated above for the compounds of general formula (I), is carried out be reacting a compound of general formula (V) R3 ~

(V) wherein R2 represents a methyl group and R3, R4 and R$ have the same meaning as that indicated above for the compounds of general formula (I), with mono-, di-or trifluoroacetic anhydride in the presence of the complex dimethyl suiphide-boron trifluoride. The reaction is carried out in a suitable solvent such as, for example, halogenated hydrocarbons such as dichloromethane, chloroform or carbon tetrachloride or ethers such as dioxane, tetrahydrofuran, ethyl ether or dimethoxyethane. The most suitable temperatures vary between -70 C and the reflux temperature of the solvent, and the reaction times lie between twenty minutes and twenty hours.

'The preparation of compounds of general formula (II), wherein R, represents a methyl or trifluorometyl group, R2 represents an hydrogen atom and R3, R4 and R5 have the same meaning as that indicated previously for the compounds of general formula (I), are carried out by different procedures among which can be found, for exarriple, the Claisen-Schmidt reaction between a benzaldehyde of general formula (IV) and acetone or 1,1,1-trifluoroacetone in presence of an aqueous solution of alkaline metal hydroxide such as sodium hydroxide or potassium hydroxide or acetic acid and piperidine; the Wittig-Horner reaction between a benzaidehyde of general formula (IV) and a 2-oxo-alkyl phosphonate in the presence of an aqueous solution of a base such as, for example, potassium carbonate or potassium bicarbonate; the reaction of a benzaldehyde of general formula (IV) witti a,a-bis(trimethylsilyl)-t-butylketimine in the presence of a Lewis acid such as zinc dibromide for example or by reaction of a compound of general formula (VI) - ci Rdl (VI) wherein R3, R4 and R5 have the same rneaning as that indicated above for the general formula (I), with trimethylaluminium in the presence of aluminium trichloride.
The reaction is carried out in a suitable solvent such as, for example, an alcohol such as methanol or ethanol, a halogenated hydrocarbon such as carbon tetrachioride, chloroform or dichloromethane, an ether such as tetrahydrofuran, ethyl ether, dioxane or dimethoxyethane, water or a mixture thereof. The reaction temperature can vary between -60 C and the refiux temperature of the solvent and the reaction times can vary between two hours and several days.

The preparation of compounds of general formula (II), wherein R, and R2 represent an hydrogen atorn and R3, R4 and R5 have the same meaning as that indicated above for the compounds of general formuia (I), are carried out following different methcds arnong which can be found, for example, the Wittig-Homer reaction with a benzaldehyde of general formula IV and then reducing the unsaturated a,(3-ester with a metal hydride such as diisobuty(aluminum hydride (Dibal); by reaction of a benzaldehyde of general formula IV with a,a-bis(trimethylsilyl)-t-butylacetaldimine in the presence of a Lewis acid such as zinc dibromide or by condensation of a benzaldehyde of general formula IV with acetaidehyde in the presence of a alkaline metal hydroxide such as sodium hydroxide or potassium hydroxide.

METHOD F
The preparation of the compounds of general formula (I), wherein R,, R2, R3, R4, R7 and R8 have the same meaning as that indicated above and one of R5 and Rs represents an atom of hydi-ogen, chlorine or fluorine, a methyl, trifluoromethyl, methoxy or trifluoromethoxy group, and the other of R5 and R13 is an acetylaminosuiphonyl group, is carried out by reacting a compound of general formula (I) wherein R,. R2, R3, R4, R7 and R8 have the same meaning as that indicated above and one of R5 and R6 represents an atom of hydrogen, chlorine or fluorine, a methyl, trifluoromethyl, methoxy or trifluoromethoxy group, and the other of R5 and R6 is an acetylaminosulphonyl group, with a suitable reactant such as, for example, acetyl chloride or acetic anhydride. The reaction is carried out in the absence of solvent, or in a suitable solvent such as, for example, dimethylformamide or pyridine. The most suitable temperatures vary between 0 C
and the rPflux temperature and the reaction times lie between 15 minutes and hours.
The invention provides pharmaceutical compositions that comprise, as well as a pharmaceutically acceptable excipierit, at least one compound of general formula (I) or a physiologically acceptable salt thereof. The invention also relates to use of a compound of general formula (I) and its physiologically acceptable < = 27395-101 salts in the preparation of a medicament for the treatment of, or for the treatment of, inflammation and/or for the treatment of other disorders associated with inflammation.
In the following examples the preparation of novel compounds according to the invention is indicated. Some typical forms of use are also disclosed for different fields of application, as well as pharmaceutical formulae applicable to the compounds of the invention. The examples that are indicated below, given by way of illustration, should not in any way limit the scope of the invention.

The invention also provides a commercial package comprising a compound, salt or composition of the invention and associated therewith instructions for the use thereof in the treatment of the above noted conditions or diseases.

Example 1 (entry 1 of the Tables).-1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(4-methylphenyl)-3-trifluoromethyl-1H-pyrazole N'N

Preparation of (E)-1,1,1-trifluoro-4-(4-methylphenyl)-3-butene-2-one (Method E-1) Into a flask with dry inert atmosphere, 15 ml of anhydrous THF is introduced and the flask cooled to -70 C. A
solution of 2 M LDA in THF-hexane (5 ml, 10 mmoles) and diethylmethyl phosphonate (0.75 ml, 5 mmoles) dissolved in 5 ml of THF are added and the flask shaken for 30 minutes.
Then, N-phenyltrifluoroacetimidoyl chloride (1.04 g, 5 mmoles) is added dropwise, (prepared according to Tamura, K.;

13a Mizukami, H. et al.; J. Org. Chem., 1993, 58, 32-35) while continuing the shaking in the same conditions for 1 hour.
P-toluenaldehyde (0.6 g, 5 mmoles) is added, the cold bath removed and the flask left with shaking at room temperature for 16 hours. 10 ml of 2N HCI are added with shaking for a further 4 hours. The THF is eliminated with a rotavapor, the mixture extracted with ethyl ether (3x20 ml) and the combined organic extracts washed with 5% sodium bicarbonate solution and with saturated sodium chloride solution until reaching a pH ~ 6. The mixture is dried over anhydrous sodium sulphate and evaporated. The crude oil obtained is purified using column chromatography through silica gel under pressure (eluting with AcOEt-petrol ether 1:9) to obtain (E)- 1,1,1-trifluoro-4-(4-methylphenyl)-3-butene-2-crc (0.8 g, yield:
Li 75%) in the form of a clear oil.
IR (film, cm-' ): 1715, 1601, 1201, 1183, 1145, 1056, 811, 703 'H-NMR (CDC13): 6 2.4 (s. 3H); 6.97 (d, J=18Hz, 1 H); 7.25 (d, J=9Hz, 2H);
7.54 (d, J=9Hz, 2H); 7.95 (d, J=18Hz, 1 H).
Thin layer chromatography (TLC) (Petrol ether): Rf=0.16 1 C) Preparation of 1-(4-aminosulphonylphenyl)-4,5-dihydro-5-(4-methylphenyl)-3-trifluoromethyl-1 H-pyrazole (METHOD A) A solution of 4-(aminosulphonyl)phenylhydrazine chlorohydrate (0.82 g, 3.69 mmoles) and (E)-1,1,1-trifluoro-4-(4-methylphenyl)-3-butene-2-one (0.79 g, 3.69 15 mmoles) in 15 ml of acetic acid is refluxed for 3 hours under a nitrogen atmosphere. It is cooled, poured over water and extracted with AcOEt. The organic solution is washed with water, dried over anhydrous sodium sulphate and evaporated to dryness under vacuum. The crude product thus obtained is crystallised from EtOH-petrol ether to give 1-(4-aminosulphonylphenyl)-4,5-20 dihydro-5-(4-methylphenyl)-3-trifluoromethyl-1 H-pyrazole (0.65 g, yield:
45%).
m.p. = 140-3 C.
IR (KBr, cm1): 3356, 3268, 1594, 1326, 1170, 1139, 1120, 1097 'H-NMR (CDCI3): 6 2.34 (s, 3H); 2.99-3.06 (dd, J=6.9 and 14 Hz; 1 H); 3.66-3.73 (dd, J=12.6 and 14 Hz, 1 H); 4.69 (broad s, 2H); 5.38-5.45 (dd, J=6.9 and 12.6 Hz, 25 1 H); 7.04-7.11 (2d, J=8.1 and 9.3 Hz, 4H); 7.17 (d, J=8.1 Hz, 2H); 7.70 (d, J=9.3 Hz, 2H).
13C-NMR (CDCI3): 20.9; 41.2; 64.5; 113.4; 120.5 (q, J=268 Hz); 125.3; 127.6;
130.1; 133.2; 136.7; 138.3; 138.8 (q, J=38 Hz); 146Ø
TLC (AcOEt): Rf=0.89 Example 2. (eritry 2 in the Tables) 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-phenyl-5-methyl-3-trifiuoromethyl-1 H-pyrazole H C "
~N
N

1 / !
SOZNHZ
5 Preparation of (E)-1,1,1-trifluoro-4-methyl-4-phenyl-3-butene-2-one (METHOD
E-2). To a solutiori of dimethyl sulphide-boron trifluoride (3.9 g, 30 mmoles) in 75 ml of dichloromethane cooled to -60 C trifluoroacetic anhydride (6.3 g, 30 mmoles) is added slowly. The mixture is shaken for 10 minutes and a solution of a-methylstyrene (3.54 g, 30 mmles) in 15 ml de dichloromethane added slowly,

10 maintaining the temperature at -600 C. Then the temperature is allowed to rise to -500 C, and kept at this value for 15 minutes, then allowed to rise to 00 C and the mixture shaken under these conditions for 30 minutes. 50 ml of ethyl ether and ml of an aqueous solution of 10% sodium bicarbonate solution are added. The phases are separated and the aqueous phase washed with more ether. The 15 combination of the ether phases is washed with water, dried over arihydrous sodium sulphate and evaporated to dryness with a rotavapor. The crude product thus obtained is purified using column chromatography through silica gel under pressure eluting with petrol ether. 2.0 g (51%) of unreacted starting a-methylstyrene and 2.35 g of (E)-1,1,1--trifluoro-4-phenyl-3-butene-2-one (yield:
75%) were recovered in the form of colourless oil.
IR (film, cm1): 1709, 1596, 1204, 1142, 1072.
'H-NMF (CDCI3): S 2.71 (s, 3H); 6.8 (s, 1H); 7.45 (m, 3H); 7.6 (m, 2H).

Preparation of 1-(4-aminosulphonylphenyl)-4,5-dihydro-5-phenyl-5-methyl-3-trifluoromethyl-1 H-pyrazole (METHOD A) In a flask with an inert atmosphere (E)-1,1,1-trifluoro-4-methyl-4-(4-methylphenyl)-3-butene-2-one (1.75 g, 8.2 mmoles), 4-(aminosulphonyl)-phenylhydrazine chlorohydrate (2 g, 9 mmoles) and piperidine (0.85 g, 10 mmoles) are added, dissolved in 100 ml of ethanol, and heated under reflux for 5.5 hours. The mixture is cooled, the rc.lvcrit eliminated with a rotavapor, water added to the residue and the solution extracted with AcOEt. The organic phase is washed with water, dried over anhydrous sodium sulphate and evaporated to dryness. The crude product is purified using column chromatography through silica gel under pressure, eluting with AcOEt-petrol ether (4:6) obtaining 1-(4-aminosulphonyiphenyl)-4,5-dihydro-5-phenyl-5-methyl-3-trifluoromethyl-1 H-pyrazole in the form of a white solid (1.46 g, yield: 47%) with a m.p.=60-6 C
IR (KBr, cm-1): 3384, 3266, 1593, 1498, 1327, 1151, 1099, 703.
'H-NMR (CDCI3): 8 1.6 (s, 3H); 2.8 (m,1 H); 3.1 (m, 1 H); 4.5 (broad s, 2H);
7.2 (m, 3H); 7.4-7.55 (m, 4H); 7.7 (d. 2H).
13C-NMR (CDCI3): 27.6; 54.2; 63.1; 114.6: 124.0 (q, J=268 Hz); 125.6; 127.4;
127.8; 129.1; 131.0; 142.0 (q, J=38 Hz). 142.6; 147.5.

Example 3 (entry 3 in the Tables).- 1-(4-aminosulphonylphenyl)-5-(2,4-difluorophenyl)-4,5-dihydro-.3-trifluoromethyi-1 H-pyrazole e;N I

N F

Preparation (E)-1,1,1-trifluoro-4-(2,4-diffuorophenyl)-3-butene-2-one (Method E-3) In a flask 2,4-difluorobenzaidehyde (20 g, 0.14 moles), glacial acetic acid (12.2 g, 0.2 moles) and piperidine (12.2 g, 0.14 moles) are dissolved in THF
(300 ml). The solution is cooled to 5-10 C and CF3COCH3 (8 g, 0.07 moles) bubbled through it. It is removed from the cold bath, the temperature increased to room temperature and the mixture kept at this temperature for 1.5 hours with continuous shaking. CF3COCH3 (5 g, 0.045 moles) is added once again and the mixture left for 1.5 hours with shaking. Once again 5 g is added and the mixture sha!,Qn for a further 1.5 hours. This step is repeated until a total of 35 g (0.31 moles) of CF3COCH3 have been added. A solution of 20% (50 ml) is added and the solvent eliminated under reduced pressure. 50 ,nl of water is added and the solution extracted with AcOEt. The organic phase is washed with water, 5% HZSOa, water and the mixture dried over anhydrous sodium sulphate. The solution is filtered and evaporated. The resulting crude product is distilled, obtaining 18.1 g of (E)-1,1,1 .-trifluoro-4-(2,4-difluorophenyl)-3-butene-2-one with a m.p. of 50-1 C.
IR (KBr, cm-1): 1717, 1602, 1583, 1277, 1146, 1059, 706 'H-NMR (CDCI3): 6 6.9 (m, ,2H); 7 05 (d, J=16 Hz, 1H); 7.6 (m, 1H); 8.0 (d, J=16 Hz, 1 H).
Preparation of 1-(4-aminosulphonylphenyf)-5-(2,4-difluorophenyl)-4,5-dihydro-3-trifluoromethyl-1 H-pyrazole (METHOD A) A solution of 4-(aminosulphonyl)phenylhydrazine chlorohydrate (47.8 g, 0.21 moles) and (E)-1,1,1-trifluoro-4-(2,4-difluorophenyl)-3-butene-2-one (53.1 g of 95%, 0.21 moles) in 315 ml of acetic acid is refluxed for 24 hours under a nitrogen atmosphere. The mixture is cooled, poured over water and filtered. It is washed with toluene and the crude product thus obtained crystallised from isopropanol.
46.2 g is obtained. The mother waters of crystallisation from crystallisation, once concentrated, give another 12.6 g of product. In total 58.8 g (68%) of 1-(4-dminosulphonylphenyl)-5-(2,4-difluorophenyl)-4,5-dihydro-3-trifluoromethyl-1 H-pyrazole with a melting point of 160-2 C.
The following procedure can also be followed:

In a flask with an inert atmosphere sodium ethoxide (0.53 g, 7.72 mrr,oles) is dissolved in 45 ml of ethanol. 1, 1, 1 -trifluoro-4-(2,4-difluorophenyl)-3-butene-2-one (prepared according to method E-1) (0.913 g, 3.86 mmoles) and 4-(aminosulphonyl)phenylhydrazine chlorohydrate (0.87 g, 3.87 mmoles) are added and the mixture was refluxed for 16 hours The mixture was cooled, evaporated to dryness, cold water added, and the mixture acidified by adding acetic acid and the precipitated solid filtered. This solid was redissolved in ether, treated with active C, filtered and the solvent eliminated with a rotavapor. The resulting residue was crystallised from ethyl ether-petrol ether (50:50) to give 1-(4-aminosulphonylphenyl)-5-(2,4-difluorophenyl)-4, 5-dihydro-3-trifluoromethyl-1 H-pyrazole (1.02 g, yield: 65%) in the form of a solid m.p.= 160-2 C.
IR (KBr, cm-1): 3315, 3232, 1617, 1593, 1506, 1326. 1179, 1099, 1067.
'H-NMR (CDCI3): S 3.0 (dd, J=6.3 and 11.4 Hz, 1 H); 3.80 (dd, J=11.4 and 12.6 Hz, 1 H); 4.79 (broad s, 2H); 5.70 (dd, J=6.3 and 12.6 Hz. 1 H); 6.8-.6.95 (m, 2H); 7.01-7.09 (m, 3H); 7.74 (d, J=8.7 Hz, 2H).

Example 4 (entry 4 of the Tables).- 4,5-dihydro-l-(4-methylphenyl)-5-(4-methylsulphonylphenyl)-3-trifluorometyl-1 H-pyrazole (METHOD A) CF

!n a flask with an inert atmosphere (E)-1,1,1-trifluoro-4-(4-methvlsulphonyiphenyl)-3-butene-2-one (prepared according to the method E-1) (1.83 g, 6.58 rnmoles) and 4-methylphenylhydrazine chlorohydrate (1.04 g, 6.58 mmoles) are dissolved in 50 ml de ethanol. A few drops of hydrochloric acid are added, and the mixture refluxed under ari inert atmosphere for 4 days. The mixture is cooled and the product crystallised. The solution is filtered and the product recrystallised from ethanol. 4,5-dihydro- 1 -(4-methylphenyl]-5-(4-methylsulphonylphenyl)-3-trifiuoromethyl--1 H-pyrazole (0.8 g, yield: 32%) is obtained in the form of a solid with a melting point of 140-3 C.
i R(KBr, cm-' ): 1516, 1310, 1148, 1131, 1060, 774 'H-NMR (CDCI3): S 2.2 (s, 3H); 2.9(~ c', J-7 8, 17.1 Hz, 1H); 3.05(s, 3H);
3.7(dd, J=12.9, 17.1 Hz, 1H); 5.45(dd, J=7.8. 12.9 Hz, 1 H); 6.8(d, J=8.4 Hz, 2H);
7(d, J=8.4 Hz, 2H); 7.45(d, J=8.4 Hz, 2H); 7.9(d, J=8.4 Hz, 2H) Example 5 (entry 39 in the Tables).- methyl 4,5-dihydro-5-(4-methylphenyl)-1-(4-methylsulphonylphenyl)-1 H-pyrazole-3-carboxylate (METHOD B) COCH
sN
H3C 15 So2cH, 4,5-dihydro-5-(4-methylphenyl)-1-(4-methylsuiphonylphenyl)-1 H- pyrazole-3-carboxylic acid (6.9 g, 19.3 mmoles) and thionyl chloride (3.5 ml, 48 mmoles) are dissolved in 50 ml of tetrahydrofuran and the mixture shaken at room temperature for 16 hours. The mixture is evaporated to dryness with a rotavapor and the crude acid chloride so obtained is dissolved ir1 150 ml of methanol in a flask with inert atmosphere, and 8 ml (58 mmoles) of triethylamine added and the mixture shaken at room temperature for 2 hours. Water is added, the solid filtered and washed with abundant water and methanol. The desired methyl ester is thus obtained (5.8 g, yield: 82%) in the form of a cream coloured solid with a m.p. =155-160 C.
IR( KBr, cm1): 1741, 1561, 1260, 1226, 1135, 1089 'H-NMR (CDC13): 2.3(s, 3H); 3(s, 3H); 3.1(dd, J=6, 18.3Hz, 1 H); 3.75(dd, J=12.6, 18.3Hz, 1 H); 5.4(dd, J=6, 12.6Hz, 1 H); 7-7.25(m, 6H); 7.7(d, J=8,7Hz, 2H) Example 6 (entry 41 in the Tables).- Preparation of 1-(4-aminosulphonyiphenyl)-4,5-dihydro-5-(4-methylphenyl)-1 H-pyrazole-3-carboxamide (METHOD C) 5 ~
_-N
.~,.
/N

1-(4-aminosulphonylphenyl)-4, 5-dihydro-5-(4-methylphenyl )-1 H-pyrazole-3-carboxylic acid (3.7 g, 10.3 mmoles) aruJ thionyl chloride (3 g, 25.8 mmoles) are dissolved in 70 ml of tetrahydrofuran and shaken at room temperature for 16 hours. The mixture is evaporated to dryriess with a rotavapor and the crude acid chloride so obtained dissolved in 30 ml of methanol in a globe of inert atniosphere and cooled to 00 C. 9 ml of concentrated ammonium hydroxide solution dissolved in 20 ml of THF is added. The mixture is shaken at room temperature for 16 hours and the solvent eliminated with the rotavapor. Water is added to the residue and the mixture extracted with ethyl acetate, which is washed with water, dried over anhydrous sodium sulphate and evaporated to dryness. The crude residue so obtained is crystallised from ethyl acetate-petrol ether to give 2.6 g(yield:
72%) of the desired compound with a m.p.=210-5 C
IR (KBr, cm-1): 3450, 3337, 1656, 1596, 1345, 1141 'H-NMR (d4-CH3OH): b 2.4(s, 3H); 3.05(dd, J=6, 17.7Hz, 1H); 3.8(dd, J=12.9, 17.7Hz, 1 H); 5.6(dd, J=6, 12.9Hz, 1 H); 7.2-7.3(m, 6H); 7.75(d, J=8.7Hz, 2H) Example 7(entrv 43 in the Tables).- Preparation of 3-cyano-4,5-dihydro-5-(4-methylphenyl)-1-(4-methylsulphonylphenyl)-1 H-pyrazole (METHOD D) CN

SO?CH3 In a flask with inert atmosphere 6.3 ml of anhydrous DMF is placed, the flask cooled to 00 C and 2.1 ml of thionyl chloride slowly added. The flask is shaken for 2 hours in these conditions. A solution of 4,5-dihydro-5-(4-methylphenyl)-1-(4-methylsuiphonyiphenyl)-1 H-pyrazole-3-carboxamide (3.8 g, 10.6 mmoles) in 30 ml of DMF is added and the rnixture shaken for 5 hours at 00 C and, then, for 16 hours at room temperature. The contents of the flask are poured onto ice and the solid precipitate filter'ed. 3.35 g (yield: 93%) of crude product are obtained which is crystallised from ethyl acetate giving a yellow solid with a m.p. =162-4 C.
IR (KBr, cm1): 2220, 1593, '1500, 1389,1296, 1143 'H-NMR (CDCI3): 8 2.3(s, 3H); 3-3.1(s+dd, 4H); 3.75(dd, J=12.6, 18Hz, 1H);
5.5(dd, J=6.3, 12.6Hz, 1 H); 7-7.2(m, 6H); 7.7(d, J=8.7Hz, 2H) Example 8(entrV 64 of ttie Tables).- 1-(4-acetylaminosulphonylphenyl)-5-(2,4-di-i:.uorophenyl)-4,5-dihydro--3-trifluoromethyl-1 H-pyrazole (METHOD F) CF, eN
eN I
F

0.58 g (1.43 mmoles) of 1-(4-aminosulphonylphenyl)-5-(2,4-difluorophenyl)-4,5-dihydro-3-trifluoromethyl-1 H-pyrazole and 2 mi of acetyl chloride are heated under reflux for 2 hours. The mixture is cooled, evaporated to dryness under reduced pressure and the resulting residue dissolved in AcOEt, washed with water. dried over Na2SO4 and evaporated to dryness. 0.49 g (76%) of 1-(4-acetylaminosulphonylpheny'd)-5 ;2,4--diflucrophenyl)-4,5-dihydro-3-trifluoromethyl-1H-pyrazole were obtained in the form of a white solid with a m.p. =172-4 C.

IR (KBr, cm-1): 3302, 1723, 1593, 1506, 1337, 1165 'H-NMR (CDC13): S 2.0 (s, 3H); 3.0 (dd, J=6.6, 18.0Hz, 1H); 3.8(dd, J=12.9, 18.0Hz, 1H); 5.7(dd, J=6.6, 12.9Hz, 1 H),; 6.9 (m. 2H); 705 (m+d, 3H); 7.85 (d, J=8.7Hz, 2H); 8.1 (s, 1 H) Examples 9 and 10 (entries 75 and 76 in the Tables).- (+)-1-(4-aminosulphonylphenyl)-5-(2,4-diffuorophenyl)-4,5-dihYdro-3-trifluoromethyl-1 H-pyrazole and (-)-1-(4-amino sulphonylphenyl)-5-(2,4-difluorophenyl)-4,5-dihydro-3-trifiuoromethyl-1 H-pyrazole CF
F H ( ,,-N
..~ N

F .~ ~

The racernic mixture 1-(4-aminosulphonylphenyl)-5-(2,4-difluorophenyl)-4,5-dihydro-3-trifluoromethyl-1 H-pyrazole is resolved into its enantiomers by high performance liquid chromatography using a CHIRALPAK AS column with 10 particles and dimensions of 21-; x 2 cm (Daicel), mobile phase 0.1 %
diethylamine in methanol and a flow rate of 3 ml/min. At a retention time of 7.4 minutes (+)-1-(4-aminosulphonylphenyl )-5-(2, 4-difluorophenyi)-4, 5-dihydro-3-trifluoromethyi-pyrazole is obtained as a white solid with a melting point of: 173-4 C;
enantiomeric purity 99.9 %; [u]0=+183.9 (c=1 CH3OH). At a retention time of 9.2 minutes (--)-1-(4-aminosulphonylphenyl)-5-(2,4-difluorophenyl)-4,5-dihydro-3-trifluoromethyl-lH-pyrazole is obtained as a white solid with a m.p.: 173-4 C;
enantiomeric purity >99,9%; [a]p=-189.4 (,c=1 CH3OH).
Following the same procedure the examples corresponding to entries 77 and 78 in the tables are obtained.

Table 1 shows some examples that are encompassed by the general formula (I) and in Table 2 the data are indicated for identification of these compounds.
The examples 1-36, 44-63 and 65-74 have been prepared according to method A, examples 37-39 according to method B, examples 40-42 according to method C, example 64 according to method F and the enantiomerically pure compounds 75-78 by resolution of the racemic rnixture.

Table I

R4 ~ N
~ R8 R5 #R7 Example R, R2 R3 R4 R5 R6 R7 R8 2 CF3 CH~ H H H SO2NH2 H H

6 CF3 H H H~ H SO2CH3 H H

8 CF3 H H H F SO?NH2 H I-i ~--9 CF3 H H H F SOZCHa H H

11 CF3 HH F F SO2NHZ H H

12 CF3 H CI H CI SO2CH3 H H

13 CF3 ~ H CI H Cl SO2NH2 H H

14 CF3 H CHs H H SO2NH2 H H

22 CF3 H H H OCF3 SOzNHz H H
23 CF3 H F F H SOzNHz H H
24 CF3 u';H~ H CH3 SOZNHz H H

26 CH3 H H H F SOZNHz H H

29 CH3 H H H CH3 SO2C1-t3 H Fi -h-- --~-----r---+---~ 33 CH3 H H H~ CF3 SO2CH3 H H

34 C02H H H HT CH3 SOzNHz H H
COzH H H H H SOzNHz H H

37 CO2CH3 H H H CHs S02NH2 H H
38 CO2CH3 H H H H SOzNHz H H
39 CO2CH3 H; H H CH3 SO2CH3 H H

41 CONH2 H H H CH3 SOzNHz H H

47 CF3 H F H OCH3 SO2NHz H H

Table 1 (continuation) 49 CF3 H OCH~ H F SO2NH2 H H

54 CF3 H CFj H CF3 SO2NH2 H H
55 CF3 H CH3 , F H S02NH2 H H

63 CF3 H FH CH3 SOzNHz H H
64 C F3 H F~-~- H F SO2NHAc H H

66 CF3 H 1-I H u S02CHJ H H H

Table I (continuation) R4 N~N

R5 #R7 Enantiom Specific rotation Example R, R2 R3 R4 R5 R6 R7 R8 eric [a]p Purity %
75 CF3 H F H F SO2NH2 H H >99 +183.9 1 c=1 ; CH3OH
76 CF3 H F H F S02NH2 H H >99 -189.4 c=1 ; CH3OH
77 CF3 H H H SO2CH3 F H H >99 +181.2 c=1 ; CH3OH
78 CF3 H H H SO2CH3 F H H >99 -183.4 _ c=1 ; CH3OH

Table 2 Exam m.p. IR (KBr) H-NMR (CDC13) ple C cm' b ppm 1 140-3 3356, 3268. 1594. 2.34 (s, 3H); 3(dd, J=6.9, 14Hz, 1 H); 3.7(dd, 1326, 1170, 1139, J=12.6, 14Hz,1H); 4.7(broad s,2H); 5.4(dd, 1 120, 1097 J=6.9, 12.6Hz,1 H); 7 1(2d, J=8.1, 9.3Hz,4H);
7.2(d,J=8.1 Hz,2H); 7.'7(d,J=9.3Hz,.2H) 2 60-6 3384, 3266. 1593, 1.6(s, 3H); 2.8(m,1 H); 3.1(m,1 H); 4.5(broad s, 1498, 1327 1151, 2H); 7.2(m, 3H); 7.4-7.5`.i(m, 4H); 7.7(d,2H) 109C;-, 703 3 160-2 3315, 3232.. 1617, 3(dd,J=6.3, 11.4Hz,1 H); 3.8(dd,J=11.4, 1593, 1506. 1326, 12.6Hz, 1 H); 4.8(broad s,2H); 5.7(dd,J=6.3, 1179, 1099, 1067 12.6Hz,1 H); 6.8-6.95(m,2H); 7-7.1(rrrn,3H);
7.7(d,J=8.7Hz,2H) 4 140-3 1516, 1310. 1148, 2.2(s,3H); 2.9(dd,J=7.8, 17.1 Hz,1 H); 3(s,3H);
1131, 1 aD60, 774 3.7(dd,J=12 9, 17.1 Hz,1 H); 5.45(dd,J=7.8, 12.9Hz,1H); 6.8(d,J=8.4Hz,2H); 7(d,J=:8.4Hz, 2H); '7.45(d,J=8.4Hz,2H); 7.9(d,J=8.4Hz,2H) 156-7 3350,3269,1596,1315 3.04(dd, J=6.6, 18Hz,1 H); 3.7(dd, J=12.9, 18 1188, 1142,1 101 Hz,1 H); 4.8(s,2H); 5.45(d(I,J=6.6, 12.9Hz,1 H);
7 0(d,J=9Hz,2H); 7.2(d,J=6.6Hz,2H);
7.3(m,3H); 7.7(d,J=9Hz,2H) 6 137-40 1595, 1333, 1297, 3.0(s,3H); 3.06(dd,J=6.6, 18Hz,1 H); 3.75(dd, 1282, 1148, 771 J=12.8, 18.1H); 5.45(dd,J=6.6, 12.6Hz,1H);
7.05(d,J=9Hz,2H); 7.2(d,J=7.8Hz,2H);
7.4(m,3H); 7.7(dõJ=9Hz,2H) 7 115-19 1592, 1332, 1148, 2.3(s,3H); 3.0(s,3H); 3.05(dd,J=6.6, 19Hz,1 H) 1133, 825, 775 3.7(dd,J=12.6, 19.1 H); 5.4(dd,J=6.6, 12.6 Hz,1 H); 7 1(2d,J=8.1, 8.7Hz,4H); 7.2((J,J=8.1 _ Hz,2H); 7.7(d,J=8.7Hz,2H) 8 154-6 3337, 3254, 1594, 3.0(dd,J=6.6, 18Hz,1 H); 3.7(dd,J=12.6, 18Hz, 1510, 1324. 1158, 1 H); 4.8(s,2H); 5.4(dd,J=6.6, 12.6Hz,1 H);
740 7.1(m,4H); 7.2(m,2H); 7.7(d,J=9Hz.,2H) 9 121-22 1592, 1509.. 1148, 3.0(s,3H); 3.05(dd,J=6.6, 17.4Hz,1H); 3.7(dd, 1120, 774 J=12.6, 17.4Hz,1H); 5.4(dd,J=6.6 and 12.6Hz, 1H); 7.0(m,4H); 7.2(m,2H); 7.7(d,J=9Hz,2H
103-5 1514, 1313, 1155, 2=9(dd,J=8.4, 17.4Hz,1 H); 3(s,3H); 3.7(dd,J=
1133, 11D61, 827 12.6, 17.4Hz,1H); 5.4(dd,J=8.4, 12.6Hz,1H);
6.9(m,4H); 7.45(d,J=8.4Hz,2H); 7.95(d,J=8.4 Hz,2H) 11 153-5 3318, 3250, 1596, 3(dd,J=6.9 and 18Hz,1H); 3.7(dd,J=12.6.18Hz, 1323, 1135, 1066 1 H); 4.7(broad s,2H); 5.4(dd,J=6.9, 12.6Hz, 1 H); 7.0(m,4H); 7.2(m, 1 H; 7.7 d,J=9Hz,2H
12 198- 1596 " 320. 1303, 2.9-3=0(dd+s,4H); 3.85(dd.J=12.6, 18.3Hz, 1H) 200 1138, 775 5=8(dd,J=6.6, 12.6Hz,1 H); 7.0(2d,J=9Hz, 3H);
7.2(d,J=9Hz,1H); 7.5(s,1H); 7.8(d,J=9Hz,2H
13 143-5 3425, 3275, 1594, 2.95(dd,J=6 3, 18.3Hz,1H); 3.8(dd,J=12.3, 1332, 1158, 1111, 18.3Hz .1 H); 4.8(s,2H); 5.8(dd,J=6.3, 12.3Hz,1H); 7.0(2d,3H); 7.2(d,J=8.7Hz,1H);
825 7.5 s,1H ; 7.7 d,J=8.1Hz,2H

14 124-6 3370, 3240, 1595, (d6-DMSO), 2.4(s,3H);2.9(dd,J=6.3, 18Hz,1 H);
1331, 1154, 1103 3.9(dd,J=13.2, 18Hz,1H); 5.9(dd,J=6.3, 13.2Hz 1 H); 6.8(broad s,1 H); 7.0(d,J=9Hz,2H); 7.1 (m,3H); 7.2 t,1H ; 7.25 d,1H ; 7.6 d,J=9Hz,2H

15 125-8 3370, 32.65, 1595, (d6-DMSO), 2.3(s,3H); 3(dd.J=6.3, 18.3Hz, 1H) 1329, 1'158, 1066 3.9(dd.J=12.6, 18.3Hz,1 H); 5.7(dd,J=6.3, 12.6Hz,1 H); 7-7.15(m,5H); 7.25(t,1 H);
7.6(d,J=9Hz,2H)

16 166-8 3330, 3239 1597, ~ 3.05(dd,J=6.3, 17.7Hz,1 H); 3.7(dd,J=12.6, 1334, 1122. 769 17=7Hz.1 H); 5.7(dd,J=6.3, 12.6Hz,1 H); 7-7.2(m,5H); 7.3(m,1 H); 7.7(d,J=9Hz,2H

17 117- 1594, 1304. 1150, 3(s,3H);3.05(dd,J=6.6, 17.1 Hz,1 H); 3.8(dd,J=
121 1119,776 12.9, 17.1 Hz,1 H); 5 75(dd,J=6.6, 12.9Hz,1 H);
7-7.2(m,5H ; 7.3 m,1 H: 7.75 d,J=9Hz,2H

18 132-3 3323, 3249, 1596, 3(dd,J=7.2, 16.8Hz,1H); 3.75(dd,J=12.9, ~ 1323, 1179. 1131, 16=8Hz,1H); 4.8(broad s,2H); 5.4(dd,J=7.2, 741 12.9Hz,1H); 6.9(d,J=9Hz, 1 H); 7.05(m,4H);
7.4 m,1 H; 7.7 d,J=9Hz,2H

19 149- 1593, 1296. 1144, 3(s+dd,4H); 3.75(dd,J=12.6, 13.8Hz,1 H);
151 965,789 5.4(dd,J=6.9, 12.6Hz,1H); 6.9-7.1(m,5H);
7.4 m,1 H; 7.7 d,J=9Hz,2H

20 125-8 3336. 3254. 1593, 3(dd,J=6.6, 18Hz,1H); 3.7(s+dd,4H);
1329, 1156. 1112 4.75(broad s,2H); 5,4(dd,J=6.6, 12.9Hz,1 H);
834 6.9(d,J=8.4Hz,2H); 7.05(d,J=8.4Hz,2H);
7.1(d,J=8.4Hz,2H_); 7.7(d,J=8.4Hz,2H

21 171-3 3376, 3239, 1593, 3(dd,J=6.9, 18.3Hz,1H); 3.75(dd,J=12.6, 1500, 1328. 1153 18=3Hz,1 H); 4.7(broad s.2H); 5.4(dd,J=6.9, 12.6Hz,1 H); 7-7.2(m,4H); 7.3(m,1 H);
7 .7 d,J=8.7Hz,2H

22 134-7 3386, 3265, 1595, (d6-DMSO): 3(dd,J=6, 18.3Hz,1H);
1259õ 1159 3.9(dd,J=12.9, 18.3Hz.1H); 5.9(dd,J=6, 12.9Hz,1 H); 7.05(d,J=8.7Hz,2H); 7.1(broad s,2H); 7.4(s,4H); 7.6(d,J=8.7Hz,2H

23 152-4 3334, 3237, 15- 95, r 3.05(dd,J=6.6, 18.6Hz,1H); 3.8(dd,J=12.9, 1331 1128, 831 18.6Hz,1 H); 4 7(broad s, 2H); 5.7(dd,J=6.6, 12.9Hz,1H); 6.8(m,1H); 7-7.2(m, 4H);
7.7 d,J=7.8Hz, 2H)

24 158- 3361, 3270, 1593, 2.3(s,3H); 2.4(s,3H); 2.9(dd,J=6.9, 17.7Hz,IH);
160 1325, 1168, 1140, :3 8(dd J=12.9, 17.7Hz,1H); 4.7(broad s, 2H);
821 5.6(dd,J=6.9, 12.9Hz,1H); 6.8-7.0(m, 4H);
_ 7.1(s,1 H); 7.7(d,J=8.4Hz,2H)

25 132-5 1595, 1325, 1281, 3(s+dd, 4H); 3.8(dd,J==6.6, 18Hz,1H);
1135. 774 5.45(dd,J=12.6, 18Hz,1H); 6.9-7.05(m, 4H);
7.2(m,1H ; 7.75 d,J=9Hz,2H

26 206-8 3329, 3215, 1593, (d6-DMSO): 2(s,3H); 2.65(dd,J=5.6, 20Hz,1H);
1509, 1333, 1155, 3.55(dd,J= 2.6, 20Hz,1 H); 5.35(dd,J=5.6, 12.6Hz,1H); 6.8(d,J=8.4Hz,2H); 6.95(s,2H);
811 I 7.1-7.25 rn,4H ; 7.5 d,J=8.4Hz,2H

27 120-3 1590, 1508, 12932.1(s,3H); 2.7(dd,J=6, 18.3Hz,1 H); 2.95(s,3H);
1141 3.5(dd,J=12, 18.3Hz,1H); 5.1(dd,J=6, 12Hz,1 H); 6.9(d,J=9Hz.,2H); 7(m,2H);
7.2 m,2H ; 7.6 d,J=9Hz,2H

28 195-7 3300, 3210, 1594, (d4-CH30H): 2(s,3H); 2.2(s,3H); 2.6(dd,J=5.4, 1509, 1330. 1157 17.7Hz,1 H); 3.5(dd,J=11.7, 17.7Hz,1 H);
5.3(dd,J=5.4, 11.7Hz,1H); 6.8(d,J=8.7Hz,2H);
6.9 s,2H ; 7.1 m,4H ; 7.5 d,J=8.7Hz,2H

29 113-7 1592, 1509, 1298, 2.1(s,3H); 2.3(s,3H); 2.7(dd,J=6.3, 20Hz,1 H);
1142, 771 2.95(s,3H); 3.5(dd,J=13, 20Hz,1H);
5.1(dd,J=6.3, 13Hz,1 H); 6.9(d,J=9Hz,2H);
7.1 m,4H ; 7.6 d,J=9Hz,2H

30 190-4 3344, 3263, 1596, (d4-CHIOH): 2.9(dd,J=6, 18.3Hz,1H); 3.7(dd, 1329, 1155. 616 J=12, 18.3Hz,1H); 5.3(dd,J=6, 12Hz,1H);
7.1(m,3H); 7.4(m,5H); 7.7(d,J=8.7Hz,2H
. _._.;_

31 206-8 1595, 1 290, 1144, 2.9(s+dd,4H); 3.6(dd,J=12.3, 18.3Hz,1H);
774 5.1(dd,J=6.3, 12.3Hz,1 H); 6.9(s,1 H);
7 d,J=9Hz,2H ; 7.3 m,5H ; 7.7 d,J=9Hz,2H

32 197- 3320, 32_50, 1594, (d5-DMSO): 2(s,3H); 2.7(dd,J=5.4, 18Hz,1H);
202 1325, 1165 3 6(dd,J=12, 18Hz,1H); 5.5(dd,J=5.4, 12Hz, ~ 1 H); 6.85(d,J=8.1 Hz,2H); 7(s,2H); 7.4(d,J=8.1 ~ Hz,2H ; 7.5 d,J=8.1 Hz,2H ; 7.7 d,J=8.1 Hz,2H

33 136-8 1595, 1512, 1325, 2.1(s,3H); 2.7(dd,J=6.3, 19Hz,1H); 3(s,3H);
1141 7 1 3.5(dd,J=12.6, 19Hz,1 H); 5.2(dd,J =6.3, 12.6Hz,1H); 6.9(d,J=8.4Hz,2H);
7.35 d,J=8.4Hz,2H ; 7.6 2d,4H

34 172-6 3304, 32.37, 1706. (d4-CH30H): 2.35(s,3H); 3.05(dd,J=6,6, 1326. 1138, 18-6Hz,1H); 3.8(dd,J=12.6, 18.6Hz,1H);
5.5(dd,J=6.6, 12.6Hz,1 H); 7.2(m, 6H), 7.7 d,J=9Hz,2H
157- 3247, 1700, 159 (d4-CH3OH): 3.1(dd,J=6, 18.3Hz,1 H);
164 1333, 1150, 1098 3.9(dd,J=12.6, 18.3Hz,1 H); 5.7(dd,J=6, _ :` 12.6Hz,1H ; 7.2-7.5 m,7H ; 7.7 d,J=8.7Hz,2H
36 202-5 1730, 1582, 1275, (d6-DMSO): 2.2(s,3H); 2.8(dd,J=6.3, 18Hz,1 H);
1206, 1134, 1087 3.05(s,3H); 3.8(dd,J=12.6, 18Hz,1H);
5.7(dd,J=6.3, 12.6Hz,1H); 7.2(m, 6H);
_ 7.7(d,J=9Hz,2H); 13.2(broad s, 1 H
37 192-7 3306, 3231, 1706, f 2=2(s,3H); 3(dd,J=6 3.18Hz,1 H); 3.2(broad s, 1324, 1158 2H); 3.65(dd,J=12.6, 18Hz,1H); 3.8(s,3H);
5.4(dd,J=6.3, 12.6Hz,1 H); 7-7.1(m,6H);
_ 7.6(d,J=8_7Hz,2H) 38 84-90 3308, 3224, 1700, (d4-CH30H): 3.1(dd,J=6, 18.3Hz,1 H);
1317, 1147, 1094 3.9(s+dd, 4H); 5.7(dd,J=6, 12.9Hz,1H); 7.2-_ 7.4(m, 7H); 7.75(d,J=8.7Hz,2H) 39 155- 1741, 1561, 1260, 2.3(s,3H): 3(s,3H); 3.1(dd,J=6, 18.3Hz,1 H);
160 1226, 1135, 1089 3.75(dd,J=12.6, 18.3Hz,1H); 5.4(dd,J=6, 12.6Hz,1H); 7-7.25(m,6H); 7.7(d,J=8.7Hz,2H
200-5 3431, 3285, 1647, (d4-CH30H); 3.1(dd,J=6, 18.3Hz,1 H); 3.9 1592, 1328, 1142 (dd,J=12_9, 18.3Hz,1H); 5.7(dd,J=6, 12.9Hz, 1 H); 7.2-7.5(m, 7H); 7.75(d,J=8.7Hz,2H) 41 210-5 3450, 3337, 1656 (d4-CH30H): 2.4(s,3H); 3.05(dd,J=6, 17.7Hz,1 1596, 1345, 1141 H); 3.8(dd,J=12.9, 17.7Hz,1H); 5.6(dd,J=6, 12.9 Hz,1H ;7.2-7.3 m,6H 7.75 d,J=8.7Hz,2H
42 128- 3440, 3200,1680, 2.3(s,3H); 3(s,3H); 3.1(dd,J=6.3.18.6Hz,1H);
132 1590, 1135 3.8(dd,J=12.6, 18.6Hz,1H); 5.4(dd,J=6.3, 12.6Hz,1H); 5.6(broad s,1H); 6.7(broad s,1H);
7-7.2(m, 6H); 7.7(d>J=8.7Hz,2H) 43 162-4 2220, 1593, 1500, 2.3(s,3H); 3-3.1(s+dd,4H); 3.75(dd,J=12.6, 1389, 1296, 1143 18Hz,1 H); 5.5(dd,J=6.3, 12.6Hz,1 H); 7-_ 7.2(m,6H); 7.7(d,J=8.7Hz,2H
44 152-5 3316, 3240. 1594, 2.2(s,6H); 3(dd,J=6.3, 18.3Hz,1H); 3.7(dd, 1323, 1178, 1121 J=12.6, 18,3Hz,1 H); 4.7(broad s,2H); 5.4(dd, 1065, 549 J=6.3, 12.6Hz,1 H); 6.95(s+d,J=7.8Hz,2H);
'7.1 (2d,J=7.8, 8.7Hz,3H); 7.7(d,J=8.7Hz,2H
45 170-5 3360, 3267, 1595, 2=2(s,3H); 3(dd,J=7,2, 18Hz,1H); 3.6-1507, 1329, 1255, 3.8(s+dd,4H); 4.6(broad s, 2H); 5.35(dd,J=7.2, ~9,619 12.9Hz,1H); 6.75(d,J=7.8Hz,1H); 7(s+d,2H);
11~ 7.1 d,J=8.7Hz,2H ; 7.7 d,J=8.7Hz,2H
46 108- 3383, 2270 1595, -~3(dd,J=6.6 18.3Hz,1H); 3.75(dd,J=12.3, 18.3 114 1519, 1329. 1277, Hz,'H); 3.9(s,3H); 5.4(dd,J=6.6, 12.3Hz,1H);
1160, 1066 6.95(m,3H); 7.05(d,J=8.7Hz,2H);
7.7 d,J=8.7Hz,2H
47 157-9 3357, 3267, 1630 3.05(dd,J=6.3 , 18Hz,1H); 3.7-3.8(s+dd, 4H);
1595, 1508, 1330, 4.8(broad s,2H); 5.7(dd,J=6.3, 12.9Hz,1H);
1264, 1158 1066 6.6-6.7(m,2H); 6.95(t,J=8.7Hz,1H);
7.05 d,J=9Hz,2H ; 7.7 d,J=9Hz,2H
Table 2 (continuation) 48 121-6 3376, 3268, 1593, 2.9(dd,J=6, 18Hz,1 H); 3.65(dd,J=12.6, 1507, 1329, 1160 1 8Hz 1 H); 3.75(s,3H); 3.85(s,3H); 4.9(s,2H);
5.65(dd,J=6, 12.6Hz,1H); 6.35(d,J=8.7Hz,1H);
6.5(s,1 H); 6.9(d,J=8.7Hz,1 H);
7 d,J=8.7Hz,2H ; 7.7 d,J=8.7Hz,2H
49 179-82 3317, 3231. 1593, (d6-DMSO): 2.95(dd,J=5.4, 18Hz,1 H); 3.7-1507, 1326, 1178 3.8(m,4H); 5.8(dd,J=5.4, 12.6Hz,1 H);
6.7(dd,J=8.1, 10.5Hz,1 H); 6.9-7.1(m,6H);
7.6 d,J=8.7Hz,2H
50 181-3 3348, 3268. 1593, 2.25(s,3H); 2.35(s,3H); 2.85(dd,J=6.9, 1321,1165 18Hz,1 H); 3.7(dd,J=12.6, 18Hz,1 H);
5.45(dd,J=6.9, 12.6Hz,1 H); 6.5(t,J=54Hz,1 H);
6.8-6.9m,4H;7s,1H;7.65d,J=9Hz,2H
51 159-61 3382, 3285. 1595, 3(dd,J=6.3, 17.7t-1z,1 H); 3.8(dd,J=12.6, 1514, 1328, 1161 17.7Hz,1 H); 4.7(s,2H); 5.7(dd,J=6.3, 12.6Hz,1H); 6.8(m,1H); 6.9(m,1H);
7 d,J9Hz,2H ; 7.75 d,J=9Hz,2H
52 167-9 3318, 3239, 1593, (d6-DMSO): 3(dd,J=6.3, 18.3Hz,1 H);
1503, 1492, 1321, 3.95(dd,12.9, 18.3Hz,1 H); 5.95(dd,J=6.3, 1068 12.9Hz,1H); 7(d,J=8.7Hz,2H); 7.1-7.2(m,4H);
7.55 d,J=8.4Hz,1 H; 7,65 d,J=8.7Hz,2H
53 170-3 3425, 3284, 1595, (d6-DMSO): 3.2(dd,J=5.7, 18Hz,1 H);
1330, 1138 3.9(dd,J=12.9, 18Hz,1H); 6(dd,J=5.7, 12.9Hz,1 H); 7.1(m,4H); 7.4-7.7(m,4H);
7.8(d,J=10.8Hz,1 H) 54 212-4 3376, 3277, 1597, 2.8(dd,J=6.3, 18.5Hz,1H); 3.7(dd,J=13, 1332, 1274, 1132 18.5Hz,1H); 5.75(dd,J=6.3, 13Hz,1H);
6.1(s,2H); 6.8(d,J=8.5Hz,2H);
7.2(d,J=8.3Hz,1H); 7.6(d,J=8.5Hz,2H);
7.651d,J=8.3Hz,1H); 7.9(s,1H) 55 193-5 3353, 3270, 159- (ds-DMSO): 2.3(s,3H); 2.9(dd,J=6.1, 1509, 1321, 1141 12.2Hz,1 H); 3.95(dd,J=12.2, 12.9Hz,1 H);
5.95(dd, J=6.1, 12.9Hz,1 H); 6.65(broad s,1 H);
7(d,J=8.8Hz,2H); 7.1-7.2(m,4H);
7 .65 d,J=8.8Hz,2H

56 148-50 3384, 3266, 1593, 2.35(s,3H); 2.9(dd,J=5.6, 18Hz,1H); 3.7-1324, 1252, 1166 3.8(m,4H); 4.9(broad peak, 2H); 5.5(dd,J=5.6, 12.6Hz,1 H); 6.6(dd, J=2.2, 8.5Hz,1 H);
_ 6.8(s,'I H ; 6.85-6.95(2d,3H); 7.7(d,J=9Hz,2H
57 157-60 3384, 3346. 3277, 3(dd,J=6.1, 17.8Hz,1H); 3.7(dd,J=12.4, 3255, 1596, 1503, 17.8Hz,1 H); 4.75(s,2H); 5.6(dd,J=6.1, 1341,1158 12.4Hz,1 H); 6.5(t.J=54Hz,1 H); 6.8-7(m,5H);
7.7(d,J=8.8Hz,2H) 58 174-7 3384, 3261, 1596, 2,95(dd,J=5.6, 17.3Hz,1H); 3.75(dd,J=12.4, 1329, 11 17 17.3Hz,1 H); 4.7(broad s, 2H); 5.8(dd,J=5.6, 12.4Hz,1 H); 6.95(d,J=8.3Hz,2H); 7.2(m,2H);
7.5 d,J=7.5Hz,1H ; 7.75 d,J=8.3Hz,2H
59 105-6 1596, 1510.. 1314, 3(s+dd, 4H) 3.6 (dd, J=12.2, 17.6Hz, 1H); 5.6 1264, 1150, 845 (dd, õ=6.2, 12.2Hz, 1H); 6.65 (t, J=9Hz, 1H);
6.75 (t, J=8Hz, 1 H); 7.35 (m, 3H); 7.8 (d, J=8.3Hz, 2H) 60 157-9 3354, 3268, 1594, 2.95(dd,J=6.6, 18.5Hz,1H); 3.85(dd,J=12.7, 1325, 1122, 753 18.5Hz,1 H); 4.8(s,2H); 5.8(dd,J=6.6, 12.7Hz,1H) 6.9-7(m,3H); 7.1-7.3(m,2H);
7.45(d,J=7.8Hz,1H); 7.7(d,J=8.6Hz,2H
61 180-5 3407, 3295, 1593, (d4-CH-,OH): 3.2(dd,J=6.3, 18.1Hz,1H);
1334, 1161 3_95(dd(J=12.9, 18.1Hz,1H); 6(dd,J=6.3, 12_9Hz,1H); 7.2(d,J=8.8Hz,2H); 7.3(m,2H);
"1.4(d,J=10.3Hz,1H); 7.8(d,J=8.8Hz,2H
62 154-60 3406, 3262, 1593.. 2.4(s,3H); 2.9(dd,J=6.6, 17.8Hz,1 H);
1330, 1155 3.75(ddJ=12.7, 17.8Hz,1H); 4.8(s,2H);
5.5(dd,J=6.6, 12.7Hz,1H); 6.8-7(m,5H);
7.7 d,J=8.8Hz,2H
63 166-7 3430, 3298, 1593, 2.3(s,3H); 3(dd,J=6.3, 18.3Hz,1H);
1508, 1334. 1161, 3.75(dd,J=12.7, 18.3Hz,1 H); 4.65(s,2H);
1123 5.7(dd,J =6.3, 12.7Hz,1 H); 6.85-7(m,3H);
7.05 d,J=8.8Hz,2H); 7.7 d,J=8.8Hz,2H
64 172-4 3302, 1722, 1593, 2(s,3H); 3(dd,J=6.6, 18Hz,1 H); 3.8(dd,J=12.9, 1506, 1337, 1165 18Hz,1H); 5.7(dd,J=6.6, 12.9Hz,1H); 6.8-6.95(m 2H); 7-7.1(m,3H); 7.85(d,J=8.7Hz,2H);
_ 8.1(s,1H) 65 117-21 1594, 1492, 1310, 2.95(dd,J=7.3, 17.8Hz,1H); 3(s,3H); 3.7(dd,J=
1257, 1154, 1063 12.7, 17.8Hz,1H); 5.45(dd,J=7.3, 12.7Hz,1H);
6.8(d,J=8.8Hz,2H); 7.1(d,J=8.8Hz,2H);
7.4(d,J=8.3Hz,2H); 7.9(d,J=8.3Hz,2H
66 114-5 1598, 1503, 1275, 2-95(dd,J=7.6, 17.8Hz,1H); 3(s,3H); 3.7(dd,J=
1156, 1079, 749 12.7, 17.8Hz,1 H); 5.45(dd,J=7.6, 12.7Hz,1 H);
6.9(rn,3H); 7.15(t,J= 7.8Hz,2H);
7.4 "d,J=8.1 Hz,2H7; 7.9 'd,J=8.1 Hz,2H
3(s+dd,4H); 3.65(dd,J= 13.1, 17,1 Hz,1 H)' 67 98-9 16Q6,1503,1317, ~
1148, 1123, 762 5.8(dd,J=7.6, 13.1 Hz,1 H); 6.9(m,2H);
7(t,J=8.1 Hz,1 H); 7.3(d,J=8.1 Hz,2H);
7.45 t,,j=8.3Hz,1 H; 7.8 d,J=8.1 Hz,2H
68 104-8 1617, 1496, 1310, 2.3(s,3H); 3(m,4H); 3.5(dd,J= 11.7, 17.1Hz, 1253, 1154, 1113, 1 H); 5.45(t,J=11.7Hz,1 H); 6.75(d,J=8.5Hz,1 H);
809 7(d,J=8.5Hz,1 H); 7.1(s,1 H); 7.45(d,J=8Hz,2H);
7.9 d,J=t3Hz,2H
69 116-7 1616, 1587, 1498, 2.9(dd,J=7,5, 16.8Hz,1H); 3(s,3H); 3.7(dd,J=
1310, 1155, 828 12.7, 16.8Hz,1H); 5.4(dd,J=7.5, 12.7Hz,1H);
6.6(m,2H); 6.7(d,J=11 Hz,1 H); 7.1(dd,J=7.6, 14.9Hz,1 H; 7.4 d,J=8Hz,2H ; 7.9 d,J=8Hz,2H

70 114-6 1597, 1315, 1149, 2.25(s,3H); 2.9(dd,J=7.6. 17.8Hz,1 H); 3(s,3H);
1072, 959 789 3.7(dd,J= 12.9, 17.8Hz,1H); 5.45(dd,J=7.6, 12.9Hz,1 H); 6.6(d,J=7.8Hz,1 H); 6.7(d,J=7.8 Hz,1H); 6.9(s,1H); 7(t,J=7.8Hz,1H);
7.45 d,J=8Hz,2H ; 7.9 d,J=8Hz,2H
71 132-3 1601, 1509, 1314, 2.2(s,3H); 2.3(s,3H); 3(m,4H); 3.5(dd,J= 11.7, 1154, 1113, 809 16.6Hz, 1 H); 5.4(t,J=11.7Hz,1 H); 6.8(m,2H);
6.9 s,1H ; 7_5(d,J=8Hz,2H); 7.85(d,J=8Hz,2H
72 2.95(s,3H); 3.15(dd,J=6.5, 17.8Hz,1 H);
3.65(dd,J= 12.7, 17.8Hz,1 H); 5.95(dd,J=6.5, 12.7Hz,1 H); 6.95(d,J=7.8Hz,1 H);
7.1(t,J=7.3Hz,1 H); 7.2(m,2H);
~ 7.35 d,J=8.3Hz,2H ; 7.8 d,J=8.3Hz,2H
73 2.3(s,3H); 3(s+dd,4H); 3.5(dd,J= 11.7, 17.8Hz,1 H); 5.5(t,J=11.7Hz,1 H); 6.85 (d,J=7.8Hz,1 H); 7(m,2H); 7.1(d,J=6.1 Hz,1 H);
7.5 d,J=8.3Hz,2H ; 7.85 d,J=8.3Hz,2H
74 103-6 1625, 1483, 1312, 3(s,3H); 3.15(dd,J=5.9, 17.8Hz, 1 H); 3.7(dd,J=
1150, 1130, 819 11.7, 17.8Hz, 1H); 5.95(dd,J=5.9, 11.7Hz,1 H);
7.05(d,J=8.8Hz,1H), 7.2(m,2H);
1 7.3 d,J=8.1 Hz,2H ; 7.8 d,J=8.1 Hz,2H
75 173-4 3330, 3250, 1617, 3(dd,J=6.3, 11.4Hz,1H); 3.8(dd,J=11.4, 1593, 1506, 1329, 12.6Hz, 1 H); 4.8(broad s,2H); 5.7(dd,J=6.3, 1121, 1099, 855 12.6Hz,1 H); 6.8-6.95(m.2H); 7-7.1(m,3H);
7.7 d,J=8.7Hz,2H
76 173-4 3330, 3250, 1617, 3(dd,J=6.3, 11.4Hz,1H); 3.8(dd,J=11.4, 1593, 1506, 1329, 12.6Hz, 1 H); 4.8(broad s,2H); 5.7(dd,J=6.3, 1121, 1 C)99, $55 12.6Hz,1 H); 6.8-6.95(m,2H); 7-7.1(m,3H);
7.7 d,J=8.7Hz,2H
77 113-5 1508, 1315, 1155, 2.9(dd,J=8.4, 17.4Hz,1H); 3(s,3H); 3.7(dd,J=
1133, 1067, 83'9 12.6, 17.4Hz,1H); 5.4(dd,J=8.4, 12.6Hz,1H);
6.9(m,4H); 7,45(d,J=8.4Hz,2H); 7.95(d,J=8.4 Hz,2H) 78 113-4 1508, 1315, 1155, 2.9(dd,J=8.4, 17.4Hz,1 H); 3(s,3H); 3.7(dd,J=
1133, 1067. 827 12.6, 17.4Hz,1 H); 5.4(dd,J=8.4, 12.6H:E,1 H);
6.9(m,4H); 7.45(d,J=8.4Hz,2H); 7.95(d,J=8.4 Hz,2H
.9 1603, 1318, 1148, 3(s,3H); 3.1(dd,J=8.8, 16.4Hz,1 H);
1060, 955, 760 3.6(dd,J=12.7, 16.4Hz,1H); 5.6(dd,J=8.8, 12.7Hz,1 H); 7(d,J=7.8Hz,1 H);
7.15(t,J=8.1Hz,1H); 7.3(t,J=8.1Hz,1H);
7.4(d,J=83Hz,2H); 7.6(d,J=7.8Hz,1 H);
7.8 d,J=8.3Hz,2H ;
The products object of the invention are potent, orally active, anti-inflammatory agents, and selective inhibitors of COX-2, with a notable analgesic activity, lack ulcerogenic effects and are very active in the experimental art,i; itis test. With a view to demonstrating these activities, by way of example, some pharmacological assays are now indicated.

Inhibition of the synthesis of prostaglandins in inflammatory exudate and mucus membrane in rat.

In this assay, as well as demonstrating the selective inhibition of COX-2, the anti-inflammatory activity is also demonstrated, along with the absence of effects on gastric prostaglandins, after oral administration. The assay was carried out by modification of a method described by C). Tofanetti et al. (Med. Sci. Res.
1989, 17, 745-746). The products under study are administered orally at an initial screening dose of 40 mg/kg. One hour after treatment the rats were anaesthetised and a sponge soaked iri carrageenan was implanted subcutaneously in the interscapular zone. Six hours after implantation the rats were sacrificed and the interscapular sponges extracted as well as gastric mucous. Next the PGE2 content was determined by immunoassay for each one of the samples, in the sponge exudate on the one hand and in the gastric mucus on the other. The inhibition of PGE2 in the infPammatory exudate demonstrates anti-inflammatory activity, both of COX-2 and COX-1 inhibitors, whereas inhibition of PGE2 in the gastric mucus is considered a COX-1 inhibitory effect.
Table 3 summaries the resuits obtained with the compound of examples 3 and in table 4 the ED-50 (effective dose-50) is shown, as well as its selectivity. It is a more potent anti-inflammatory that the reference product.

TABLE 3.- COX-2/COX-1 activity in vivo Inhibition of PGE2 Product (Dose 40 mg/kg, po) Inflammatory exudatc Gastric mucus Example 3 92% 0 Meloxicam 97% 65%
Nabumetone 93% 0 TABLE 4. - ED-50 of the COX-2/COX-1 activity in vivo Product Inhibition of PGE2 ED-50 (mg/kg, po) Inflammatory exudate Gastric mucus Example 3 >40 Nabumetone 11.0 >40 Analgesic activity against "hyperalgesia" by thermal stimulus of pre-inflamed rat paw.

In this assay the analgesic activity in rat was monitored following the method 10 described by K. Hargreaves et al. (Pain, 1988, 32, 77-78). Firstly, a suspension of carrageenan was injected into the back right paw of each rat. After two hours the products under study were administered orally at a screening dose of 40 mg/kg.
Two hours after treatment a heat source was applied to the sole of each back paw of the rats and the time measured that they took to remove the paw measured.
15 Hyperalgesia was determined by comparing th3 percentage of algesia of the paw injected with carrageenan to the other back paw. The analgesic activity was calculated comparing these hyperalgesia values of the groups treated with product with those of the group treated with the vehicle only.
In table 5 the results obtained with the compound of example 3 and 20 summarised and in table 6 the ED-50 is presented, showing that this product is more active that other selective inhibitors of COX-2 in the assay of activity against thermal hyperalgesia.

TABLE 5. - Analgesic activity against hyperalgesia by thermal stimulus.
Product % Activity (Dose = 40 mg/kg, po) Example 3 100%
Nimesulide 97%
Nabumetone 95%

TABLE 6. -ED-50 of analgesic activity against hyperalgesia by thermal stimulus.
Product ED-50 (mg/kg, po) Example 3 0.2 Nimesulide 1 _0 Nabumetone 2.1 Gastrointestinal effects (GI) : induction of ulcers in rats submitted to cold stress.

In this assay possible ulcerogenic effects at a gastrointestinal level were determined after oral administration. To do this a modification of the method described by K. D. Rainsford (Agents and actions, 1975, 5, 553-558) was followed. Firstly the rats received the products under study orally at different doses. After two hours had elapsed the rats were placed in a chest freezer at -C for 1 hour. Afterwards they were left for 1 hour at room temperature. The animals were then sacrificed and the stornach extracted. The stomach was kept in saline solution for 15 minutes. After this time the percentage of surface area with gastric ulcers was determined using a Project C.S.V. vs 1.2 image analyser for each stomach. For each product the maximum dose that did not lead to ulcerogenesis was determined by linear regression analysis of the dose-response.

The results obtained with the compound of example 3 are summarised in table 7. It has been shown not to have ulcerogenic effects, even at very high doses, as was to be expected from a COX-2 selective product. On the other hand, dichlophenac and pirlo;;;cuõs, both selective COX-1 inhibitors, exhibited ulcerogenic effects at very low doses.

TABLE 7. -Induction of ulcers in rats submitted to cold stress.
Product Maximum non-Ulcerogenic dose (mg/kg, po) Example 3 >80 Dichlophenac 1.2 Piroxicam 1.7 Anti-arthritic activity in rat In this study the anti-arthritic activity in rat of the compound of example 3 has been studied. To do so the method described by B. J. Jaffee et al. (Agents and Actions, 1989, 27, 344-346) was followed_ Firstly, the Freund adjuvant was injected (Mycobacterium butiricum suspended in soy-bean oil) through the sub-scle of the back left paw of the rats. After 14 days, when the secondary inflammation had developed in the uninjected paw, which is considered the experimental arthr;tis, treatment with the product under study or with the vehicle for the control group was started. The compound of example 3 was administered orully at a dose of 10 mg/kg/day for 11 days. The volume of the paw with secondary inflammation in the last days of treatment was measured. The anti-arthritic activity was calculated by comparing the average volume of the paw with secondary inflammation of the group treated with the compound of exampNe 3 and the control group for 5 days.

The results obtained show that the compound of example 3 has a high anti-arthritic activity, as treatment with 10 mg/kg/day, po, led to an inhibition of secondary inflammation, i.e. of an anti-arthritic activity, of 71 %.

On the basis of their good pharmacodynamic properties, the derivatives of pyrazolines iri accordance with the invention, can be used in satisfactory manner in human and animal therapy, in particular as anti-inflammatory agents for the treatment of inflammation and for the treatment of other disorders associated with inflammation, such as anti-arthritics, analgesics for the treatment of pain and migraine, or as antipyretics in the treatment of fever.
In human therapy, the administration dose of the compounds of the present invention varies as a function of the seriousness of the affliction to treat.
Normally the dose will lie between 100 and 400 mg/day. The compounds of the invention '15 will be administered, for example, in the form of capsules, tablets, or injectable solutions or suspensions.
Below, by way of example, two pharmaceutical compositions containing the compounds object of the present invention are shown.

Pharmaceutical formulations Example of forrnula per tablet:

Example 3 50 mg Corn flour 16 mg Colloidal silicon dioxide 1 mg Magnesium stearate 1 rrmg Povidone K-90 3 mg Pre-gelatinised starch 4 mg Micro-crystalline cellulose 25 mg Lactose 200 mg Example of forrnula for capsule:

Example 3 100 mg Corn flour 20 mg Colloidal silicon dioxide 2 mg Magnesium stearate 4 mg Lactose 200 mg

Claims (28)

CLAIMS:

1. A derivative of pyrazoline of general formula (I):
wherein:

R1 represents a hydrogen atom, or a methyl, fluoromethyl, difluoromethyl, trifluoromethyl, carboxylic acid, lower carboxylate of 1 to 4 carbon atoms, carboxamide or cyano group;

R2 represents a hydrogen atom or a methyl group;
R3, R4, R7 and R8, identical or different, represent an atom of hydrogen, chlorine or fluorine, or a methyl, trifluromethyl or methoxy group;

one of R5 and R6 represents an atom of hydrogen, chlorine or fluorine, or a methyl, trifluromethyl, methoxy or trifluoromethoxy group, and the other of R5 and R6 represents a methylsulphonyl, aminosulphonyl or acetylaminosulphonyl group;

with the proviso that when R1 represents a methyl group, then:

R2 represents a hydrogen atom or a methyl group, R3 and R8, identical or different, represent an atom of hydrogen, chlorine or fluorine, or a methyl or trifluoromethyl group, R4 represents a hydrogen or fluorine atom, or a methyl, trifluoromethyl or methoxy group, R5 represents a fluorine atom, or triflouromethyl, trifluoromethoxy, methylsulphonyl or aminosulphonyl group, R6 represents a hydrogen, chlorine or fluorine atom, or a methyl, trifluoromethyl, methoxy, trifluoromethoxy, methylsulphonyl or aminosulphonyl group, with the proviso that one or both R5 and R6 represents a methylsulfonyl or aminosulphonyl group; and R7 represents a hydrogen, chlorine or fluorine atom, or a methyl, trifluoromethyl or methoxy group;

and a physiologically acceptable salt thereof.

2. The derivative according to claim 1, selected from the following group consisting of:

[1] 1-(4-Aminosulfonylphenyl)-4,5-dihydro-5-(4-methylphenyl) -3-trifluoromethyl-1H-pyrazole;

[2] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-methyl-5-(4-methylphenyl)-3-trifluoromethyl-1H-pyrazole;
[3] 1-(4-Aminosulphonylphenyl)-5-(2,4-difluorophenyl)-4,5-dihydro-3-trifluoromethyl-1H-pyrazole;

[4] 4,5-Dihydro-1-(4-methylphenyl)-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[5] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-phenyl-3-trifluoromethyl-1H-pyrazole;
[6] 4,5-Dihydro-5-phenyl-1-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;

[7] 4,5-Dihydro-5-(4-methylphenyl)-1-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[8] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(4-fluorophenyl)-3-trifluoromethyl-1H-pyrazole;
[9] 4,5-Dihydro-5-(4-fluorophenyl)-1-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[10] 4,5-Dihydro-1-(4-fluorophenyl)-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;

[11] 1-(4-Aminosulphonylphenyl)-5-(3,4-difluorophenyl)-4,5-dihydro-3-trifluoromethyl-1H-pyrazole;
[12] 5-(2,4-Dichlorophenyl)-4,5-dihydro-1-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole ;

[13] 1-(4-Aminosulphonylphenyl)-5-(2,4-dichlorophenyl)-4,5-dihydro-3-trifluoromethyl-1H-pyrazole;

[14] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(2-methylphenyl)-3-trifluoromethyl-1H-pyrazole, [15] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(3-methylphenyl)-3-trifluoromethyl-1H-pyrazole;
[16] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(2-fluorophenyl)-3-trifluoromethyl-1H-pyrazole ;
[17] 4,5-Dihydro-5-(2-fluorophenyl)-1-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H- pyrazole;
[18] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(3-fluorophenyl)-3-trifluoromethyl-1H-pyrazole ;
[19] 4,5-Dihydro-5-(3-fluorophenyl)-1-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[20] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(4-methoxyphenyl)-3-trifluoromethyl-1H-pyrazole ;
[21] 1-(4-Aminosulphonylphenyl)-5-(3-chloro-4-fluorophenyl)-4,5-dihydro-3-trifluoromethyl-1H-pyrazole;
[22] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-3-trifluoromethyl-5-(4-trifluoromethoxyphenyl)-1H-pyrazole;
[23] 1-(4-Aminosulphonylphenyl)-5-(2,3-difluorophenyl)-4,5-dihydro-3-trifluoromethyl-1H-pyrazole;
[24] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(2,4-dimethylphenyl)-3-trifluoromethyl-1H-pyrazole;
[25] 5-(3,4-Difluorophenyl)-4,5-dihydro-1-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[26] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(4-fluorophenyl)-3-methyl-1H-pyrazole;
[27] 4,5-Dihydro-5-(4-fluorophenyl)-3-methyl-1-(4-methylsulphonylphenyl)-1H-pyrazole;
[28] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-3-methyl-5-(4-methylphenyl)-1H-pyrazole;

[29] 4,5-Dihydro-3-methyl-5-(4-methylphenyl)-1-(4-methylsulphonylphenyl)-1H-pyrazole;
[30] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-3-methyl-5-(4-trifluoromethylphenyl)-1H-pyrazole;
[31] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-phenyl-1H-pyrazole;
[32] 4,5-Dihydro-5-phenyl-1-(4-methylsulphonylphenyl)-1H-pyrazole;
[33] 4,5-Dihydro-3-methyl-1-(4-methylsulphonylphenyl)-5-(4-trifluoromethylphenyl)-1H-pyrazole;
[34] 1-(4-aminosulphonylphenyl)-4,5-dihydro-5-(4-methylphenyl)-1H-pyrazole-3-carboxylic acid, [35] 1-(4-aminosulphonylphenyl)-4,5-dihydro-5-phenyl-1H-pyrazole-3-carboxylic acid;
[36] 4,5-dihydro-5-(4-methylphenyl)-1-(4-methylsulphonylphenyl)-1H-pyrazole-3-carboxylic acid;
[37] Methyl 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(4-methylphenyl)-1H-pyrazole-3-carboxylate;
[38] Methyl 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-phenyl-1H-pyrazole-3-carboxylate;
[39] Methyl 4,5-Dihydro-5-(4-methylphenyl)-1-(4-methylsulphonylphenyl)-1H-pyrazole-3-carboxylate;
[40] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-phenyl-1H-pyrazole-3-carboxamide;

[41] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(4-methylphenyl)-1H-pyrazole-3-carboxamide, [42] 4,5-Dihydro-5-(4-methylphenyl)-1-(4-methylsulphonylphenyl)-1H-pyrazole-3-carboxamide;

[43] 3-Cyano-4,5-dihydro-5-(4-methylphenyl)-1-(4-methylsulphonylphenyl)-1H-pyrazole, [44] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(3,4-dimethylphenyl)-3-trifluoromethyl-1H-pyrazole, [45] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(3-methyl-4-methoxyphenyl)-3-trifluoromethyl-1H-pyrazole;
[46] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(3-fluoro-4-methoxyphenyl)-3-trifluoromethyl-1H-pyrazole, [47] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(2-fluoro-4-methoxyphenyl)-3-trifluoromethyl-1H-pyrazole, [48] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(2,4-dimethoxyphenyl)-3-trifluoromethyl-1H-pyrazole, [49] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(4-fluoro-2-methoxyphenyl)-3-trifluoromethyl-1H-pyrazole;
[50] 1-(4-Aminosulphonylphenyl)-3-difluoromethyl-4,5-dihydro-5-(2,4-dimethylphenyl)-1H-pyrazole;
[51] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(2,3,4-trifluorophenyl)-3-trifluoromethyl-1H-pyrazole;
[52] 1-(4-Aminosulphonylphenyl)-5-(2-chloro-4-fluorophenyl)-4,5-dihydro-3-trifluoromethyl-1H-pyrazole;
[53] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(2-fluoro-4-trifluoromethylphenyl)-3-trifluoromethyl-1H-pyrazole;
[54] 1-(4-Aminosulphonylphenyl)-5-[2,4-(bistrifluoromethyl)phenyl]-4,5-dihydro-3-trifluoromethyl-1H-pyrazole;
[55] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(2-methyl-3-fluorophenyl)-3-trifluoromethyl-1H-pyrazole;

[56] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(2-methyl-4-methoxyphenyl)-3-trifluoromethyl-1H-pyrazole;

[57] 1-(4-Aminosulphonylphenyl)-5-(2,4-difluorophenyl)-3-difluoromethyl-4,5-dihydro-1H-pyrazole;
[58] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(4-fluoro-2-trifluoromethylphenyl]-3-trifluoromethyl-1H-pyrazole;
[59] 1-(2,4-Difluorophenyl)-4,5-dihydro-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole, [60] 1-(4-Aminosulphonylphenyl)-5-(2-chlorophenyl)-4,5-dihydro-3-trifluoromethyl-1H-pyrazole;
[61] 1-(4-Aminosulphonylphenyl)-5-(4-chloro-2-fluorophenyl)-4,5-dihydro-3-trifluoromethyl-1H-pyrazole, [62] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(4-fluoro-2-methylphenyl]-3-trifluoromethyl-1H-pyrazole;
[63] 1-(4-Aminosulphonylphenyl)-4,5-dihydro-5-(2-fluoro-4-methylphenyl]-3-trifluoromethyl-1H-pyrazole;
[64] 1-(4-Acetylaminosulphonylphenyl)-5-(2,4-difluorophenyl)-4,5-dihydro-3-trifluoromethyl-1H-pyrazole;
[65] 1-(4-Chlorophenyl)-4,5-dihydro-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[66] 4,5-Dihydro-1-phenyl-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[67] 4,5-Dihydro-1-(2-fluorophenyl)-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[68] 1-(4-Chloro-2-methylphenyl)-4,5-dihydro-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[69] 4,5-Dihydro-1-(3-fluorophenyl)-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[70] 4,5-Dihydro-1-(3-methylphenyl)-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[71] 4,5-Dihydro-1-(2,4-dimethylphenyl)-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[72] 1-(2-Chlorophenyl)-4,5-dihydro-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[73] 4,5-Dihydro-1-(2-methylphenyl)-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[74] 1-(2,4-Dichlorophenyl)-4,5-dihydro-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;

[75] (+) -1-(4-Aminosulphonylphenyl) -5- (2, 4-difluorophenyl) -4,5-dihydro-3-trifluoromethyl-1H-pyrazole;
[76] (-) -1- (4-Aminosulphonylphenyl)-5-(2,4-difluorophenyl)-4,5-dihydro-3-trifluoromethyl-1H-pyrazole;
[77] (+) -4,5-Dihydro-1-(4-fluorophenyl)-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[78] (-) -4, 5-Dihydro-1-(4-fluorophenyl)-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1H-pyrazole;
[79] 4,5-Dihydro-5-(4-methylsulphonylphenyl)-3-trifluoromethyl-1-(2-trifluoromethylphenyl)-1H-pyrazole;

and a physiologically acceptable salt thereof.

3. A process for preparing the derivative of pyrazoline of the general formula (I) according to claim 1, comprising:
reacting a compound of general formula (II):

wherein R1 represents a hydrogen atom, or a methyl, fluoromethyl, difluoromethyl, trifluoromethyl or carboxylic acid group, and R2, R3, R4 and R5 are as defined in claim 1, with a phenylhydrazine of general formula (III) in base or salt form:

wherein R6, R7 and R8 are as defined in claim 1.

4. A process for the preparation of the derivative of pyrazoline of the general formula (I) according to claim 1, wherein R1 represents a carboxylate of a lower alkyl with 1 to 4 carbon atoms, and R2, R3, R4, R5, R6, R7 and R8 are as defined in claim 1, comprising: reacting the derivative of the general formula (I), wherein R1 represents a carboxylic acid group (COOH), and R2, R3, R4, R5, R6, R7 and R8 are as defined in claim 1, with a reagent to form the acid chloride, and then carrying out an esterification reaction with an aliphatic alcohol of 1 to 4 carbon atoms in the presence of an organic base, or by direct reaction of the carboxylic acid group with the corresponding anhydrous alcohol saturated with gaseous hydrogen chloride.

5. The process according to claim 4, wherein the acid chloride is thionyl chloride or oxalyl chloride, and the organic base is triethylamine or pyridine.

6. A process for the preparation of the derivative of pyrazoline of the general formula (I) according to claim 1, wherein R1 represents a carboxamide group, and R2, R3, R4, R5, R6, R7 and R8 are as defined in claim 1, comprising: reacting the derivative compound of the general formula (I), wherein R1 represents a carboxylic acid group (COOH), and R2, R3, R4, R5, R6, R7 and R8 are as defined in claim 1, with a reagent for forming the corresponding acid chloride, and then reacting with ammonia.

7. The process according to claim 6, wherein the acid chloride is thionyl chloride or oxalyl chloride.

8. A process for the preparation of the derivative of pyrazoline of the general formula (I) according to claim 1, wherein R1 represents a cyano group, and R2, R3, R4, R5, R6, R7 and R8 are as defined in claim 1, comprising: reacting the derivative of the general formula (I), wherein R1 represents a carboxamide group, and R2, R3, R4, R5, R6, R7 and R8 are as defined in claim 1, with a reagent for forming the corresponding cyano derivative.

9. The process according to claim 8, wherein the reagent is the complex dimethylformamide-thionyl chloride or methanosulphonyl chloride.

10. A process for the preparation of the derivative of pyrazoline of the general formula (I) according to claim 1, wherein R1, R2, R3, R4, R5, R7 and R8 are as defined in claim 1, and R6 represents an acetylaminosulphonyl group, or R1, R2, R3, R4, R6, R7 and R8 are as defined in claim 1, and R5 represents an acetylaminosulphonyl group, comprising: reacting the derivative of the general formula (I), wherein R1, R2, R3, R4, R5, R7 and R8 are as defined in claim 1, and R6 represents an aminosulphonyl group, or R1, R2, R3, R4, R6, R7 and R8 are as defined in claim 1, and R5 represents an aminosulphonyl group, with a reagent for forming the corresponding acetylaminosulphonyl derivative.

11. The process according to claim 10, wherein the reagent is acetyl chloride or acetic anhydride.

12. A process for the preparation of an enantiomerically pure derivative of pyrazoline of the general formula (I) according to claim 1, comprising: effecting the resolution of a racemic mixture of the derivative of the general formula (I) by chromatography with a chiral stationary phase, or formation of a salt with an enantiomerically pure acid.

13. A process for the preparation of a physiologically acceptable salt of the derivative of pyrazoline of the general formula (I) according to claim 1, comprising reacting the derivative of the general formula (I) with an inorganic acid or with an organic acid in the presence of a solvent.

14. A pharmaceutical composition, comprising at least one derivative of pyrazoline of the general formula (I), or a physiologically acceptable salt thereof, according to claim 1 or 2, and a pharmaceutically acceptable excipient.

15. Use of the derivative of pyrazoline of the general formula (I), or a physiologically acceptable salt thereof, according to claim 1 or 2, or the composition according to claim 14, in the manufacture of a medicament for the treatment of inflammation and for the treatment of disorders associated with inflammation and processes mediated by cyclooxygenase-2 or of those processes wherein benefit is derived by inhibition of cyclooxygenase-2 in mammals.

16. Use of the derivative of pyrazoline of the general formula (I), or a physiologically acceptable salt thereof, according to claim 1 or 2, or the composition according to claim 14, for the treatment of inflammation and for the treatment of disorders associated with inflammation and processes mediated by cyclooxygenase-2 or of those processes wherein benefit is derived by inhibition of cyclooxygenase-2 in mammals.

17. The use according to claim 15 or 16, for the treatment of arthritis in mammals.

18. The use according to claim 15 or 16, for the treatment of pain in mammals.

19. The use according to claim 15 or 16, for the treatment of fever in mammals.

20. The derivative of pyrazoline of the general formula (I), or a physiologically acceptable salt thereof, according to claim 1 or 2, or the composition according to claim 14, for use in the manufacture of a medicament for the treatment of inflammation and for the treatment of disorders associated with inflammation and processes mediated by cyclooxygenase-2 or of those processes wherein benefit is derived by inhibition of cyclooxygenase-2 in mammals.

21. The derivative of pyrazoline of the general formula (I), or a physiologically acceptable salt thereof, according to claim 1 or 2, or the composition according to claim 14, for use in the treatment of inflammation and for the treatment of disorders associated with inflammation and processes mediated by cyclooxygenase-2 or of those processes wherein benefit is derived by inhibition of cyclooxygenase-2 in mammals.

22. The derivative, salt or composition according to claim 20 or 21, for the treatment of arthritis in mammals.

23. The derivative, salt or composition according to claim 20 or 21, for the treatment of pain in mammals.

24. The derivative, salt or composition according to claim 20 or 21, for the treatment of fever in mammals.

25. A commercial package comprising the derivative of pyrazoline of the general formula (I), or a physiologically acceptable salt thereof, according to claim 1 or 2, or the composition according to claim 14, and associated therewith instructions for the use thereof in the treatment of inflammation and for the treatment of disorders associated with inflammation and processes mediated by cyclooxygenase-2 or of those processes wherein benefit is derived by inhibition of cyclooxygenase-2 in mammals.

26. The commercial package according to claim 25, in the treatment of arthritis in mammals.

27. The commercial package according to claim 25, in the treatment of pain in mammals.

28. The commercial package according to claim 25, in the treatment of fever in mammals.